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VARIANTnbs Newborn Hemoglobin Screening System
The VARIANTnbs is the established worldwide standard in automated newborn screening for sickle cell disease and other hemoglobin disorders. It features fully automated analysis and advanced result reporting for maximum efficiency. Using dried blood spot specimens, the VARIANTnbs identifies the most clinically significant hemoglobin variants, including hemoglobins F, S, A, C, D and E, as well as the carrier status for abnormal hemoglobin variants and many double-heterozygote conditions. The VARIANTnbs provides the total hemoglobin picture.
